Jobs at Biogen

Provides strategic clinical quality and compliance leadership across R&D, including QMS governance, clinical study oversight, risk management, investigations, CAPA, vendor quality governance, audits, regulatory inspections, and continuous improvement. Advises cross-functional teams on GCP and global regulatory requirements while strengthening inspection readiness, data integrity, patient safety, and quality performance.

Supports early-phase immunology and neuroimmunology clinical development programs, including protocol design, trial execution, medical monitoring, data interpretation, regulatory interactions, safety planning, and clinical documentation. Partners with cross-functional R&D teams, CROs, investigators, and external stakeholders while providing therapeutic expertise and monitoring developments in autoimmune disease.

Leads observational epidemiology research, including cohort, registry-based, and database studies, supporting disease understanding and post-market safety. Reviews epidemiological literature, estimates disease incidence, prevalence, progression, and risk factors, and contributes to regulatory activities such as safety reports, pharmacovigilance, and risk management plans. Collaborates cross-functionally on evidence-generation planning and delivers epidemiologic expertise for clinical development, safety, medical, and value-access decisions.

Leads enterprise architecture for Biogen’s Veeva ecosystem across Development, Quality, Regulatory, Safety, and Commercial functions. Translates business needs into scalable Veeva configurations and integrations, governs target-state architecture and platform standards, reviews solution designs, and oversees implementation and release planning. Mentors configuration teams, drives cross-vault consistency, manages architecture governance, aligns with Veeva product roadmaps, and advises IT leadership on platform strategy, investments, regulatory compliance, and business objectives.

Leads the architecture, implementation, and governance of enterprise IAM and IGA solutions using SailPoint and ServiceNow. Designs integrations, provisioning workflows, access certifications, role management, and segregation-of-duties controls across enterprise systems. Provides technical leadership, conducts design reviews, mentors IAM teams, leads workshops, manages risks, and ensures GxP, SOX, security, compliance, and audit requirements are met.

Lead biostatistical efforts in clinical research, oversee analysis plans, mentor junior staff, and ensure statistical integrity. Key role in data analysis and regulatory submissions.

Provide country-level clinical operational and scientific leadership to support global study execution. Liaise with investigators, CROs, sites, and internal teams; oversee sponsor oversight activities, audits, and inspections; drive site selection and monitoring; resolve local challenges; and align country strategy with global programs while promoting quality, patient safety, and operational excellence.

Support the Country and Site Lead by providing local operational and scientific expertise to inform clinical development strategy. Act as single point of contact for CROs, affiliates, and global teams; drive site engagement, monitor country performance (KPIs), support site selection, resolve investigator/site issues, and oversee sponsor oversight activities. Field-based role with heavy travel to enable trial delivery and quality.